510(k) K072070 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PHILIPS MP2 AND X2 INTELLIVUE PATIENT MONITORS
| Applicant | Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, Aug 10, 2007 |
| Received | Jul 30, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072070
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.